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Diseases
Genes (1365)
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RB1
Pinealoblastoma
Trilateral Retinoblastoma
Retinoblastoma
ABHD5
Cerebral Creatine Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
MED12
Social (Pragmatic) Communication Disorder
Fg Syndrome
PQBP1
Renpenning's Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
DMPK
Myotonic Dystrophy
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
Retinoblastoma
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis
AR
Alopecia, Androgenetic, 1
Retinoblastoma
SRD5A2
Alopecia, Androgenetic, 1